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Concise review: Dedifferentiation meets cancer development: Proof of concept for epigenetic cancer

机译:简要评论:去分化遇到癌症发展:表观遗传学概念的证明

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The technology for generation of induced pluripotent stem cells (iPSCs) has made significant contributions to various scientific fields, and the field of cancer biology is no exception. Although cancer is generally believed to develop through accumulation of multiple genetic mutations, there is increasing evidence that cancer cells also acquire epigenetic abnormalities during development, maintenance, and progression. Because the epigenetic status of somatic cells changes dynamically through reprogramming, iPSC technology can be utilized to actively and globally alter the epigenetic status of differentiated cells. Using this technology, a recent study has revealed that some types of cancer can develop mainly through disruption of the epigenetic status triggered by dedifferentiation. In this paper, we outline the reprograming process and the epigenetic mechanismassociated with the maintenance or conversion of cell identity. Wethen describe several observations suggesting that dedifferentiationcanplay an important roleincancer development. Finally,weintroducethe systemresponsible for in vivo reprogramming to demonstrate the involvement of dedifferentiation-driven epigenetic disruption in cancer development, and propose that particular types of cancer can develop predominantly through epigenetic alterations.
机译:诱导多能干细胞(iPSC)的产生技术在各个科学领域做出了重大贡献,癌症生物学领域也不例外。尽管通常认为癌症是通过多种基因突变的积累而发展的,但越来越多的证据表明,癌细胞在发育,维持和发展过程中也会获得表观遗传异常。由于体细胞的表观遗传状态通过重新编程而动态变化,因此iPSC技术可用于主动和全局地改变分化细胞的表观遗传状态。使用这项技术,最近的一项研究表明,某些类型的癌症可以主要通过去分化触发的表观遗传状态的破坏而发展。在本文中,我们概述了重新编程过程和与细胞身份的维持或转化相关的表观遗传机制。 Wethen描述了一些观察结果,表明去分化可以在增加癌症的发展中发挥重要作用。最后,我们引入了负责体内重编程的系统,以证明去分化驱动的表观遗传学破坏参与癌症发展,并提出特定类型的癌症可以主要通过表观遗传学改变发展。

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